Li Jianwei, Huang Shaohui, Huang Weiliang, Wang Wanshan, Wen Ge, Gao Lei, Fu Xiuqiong, Wang Mengmeng, Liang Weihai, Kwan Hiu Yee, Zhao Xiaoshan, Lv Zhiping
School of Traditional Chinese Medicine, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Experimental Animal Center, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Oncotarget. 2017 Jan 31;8(5):8264-8282. doi: 10.18632/oncotarget.14160.
Long-term treatment with high-dose Interferon-alpha (IFN-α) has resulted in depression in 30-50% of the patients. Paeoniflorin may ameliorate the IFN-α-induced depression; however, the underlying mechanism is less studied. Here, we investigated the prophylactic antidepressant and anti-neuroinflammatory effects of paeoniflorin on the behaviors and specific emotion-related regions of the brain in mice with IFN-α-induced depression. A series of behavior assessments were conducted to identify the depressive state after subcutaneously IFN-α injections and with or without intragastrically paeoniflorin administration in C57BL/6J mice. Levels of many inflammatory-related cytokines in serum, mPFC, vHi and amygdala were determined by cytokine array analysis. Furthermore, microglia and astrocyte activation in these three regions were evaluated by immunohistochemistry. We found that the mice which were subcutaneously injected IFN-α 15×106 IU/kg for 4 successive weeks to mimic an IFN-α-induced depression model had distinct inflammatory changes in the amygdala. Interestingly, 4-week 20 mg/kg or 40 mg/kg paeoniflorin pretreatments reversed the depressive-like behaviors and the abnormal inflammatory cytokine levels in the serum, mPFC, vHi and amygdala. These cytokines were not limited to the commonly reported IL-6, IL-1β and TNF-α, but also IL-9, IL-10, IL-12, and MCP-1. Besides, the increased density of microglia in IFN-α-treated mice was reversed by paeoniflorin in these three brain areas. Taken together, our data suggest that paeoniflorin can reverse the long-term, high-dose IFN-α-induced depressive-like behaviors that were associated with local distinct neuroinflammation in the mPFC, vHi and particularly the amygdala. Paeoniflorin might have a preventive therapeutic potential in IFN-α-induced depression.
长期大剂量使用α-干扰素(IFN-α)治疗导致30%至50%的患者出现抑郁。芍药苷可能改善IFN-α诱导的抑郁;然而,其潜在机制的研究较少。在此,我们研究了芍药苷对IFN-α诱导的抑郁小鼠行为及大脑特定情绪相关区域的预防性抗抑郁和抗神经炎症作用。对C57BL/6J小鼠皮下注射IFN-α并给予或不给予芍药苷灌胃后,进行了一系列行为评估以确定抑郁状态。通过细胞因子阵列分析测定血清、内侧前额叶皮质(mPFC)、腹侧海马(vHi)和杏仁核中多种炎症相关细胞因子的水平。此外,通过免疫组织化学评估这三个区域中小胶质细胞和星形胶质细胞的激活情况。我们发现,连续4周皮下注射15×106 IU/kg IFN-α以模拟IFN-α诱导的抑郁模型的小鼠,杏仁核有明显的炎症变化。有趣的是,连续4周给予20 mg/kg或40 mg/kg芍药苷预处理可逆转血清、mPFC、vHi和杏仁核中的抑郁样行为及异常炎症细胞因子水平。这些细胞因子不仅限于常见报道的白细胞介素-6(IL-6)?白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α),还包括白细胞介素-9(IL-9)?白细胞介素-10(IL-10)?白细胞介素-12(IL-12)和单核细胞趋化蛋白-1(MCP-1)。此外,芍药苷可逆转IFN-α处理小鼠在这三个脑区中增加的小胶质细胞密度。综上所述,我们的数据表明,芍药苷可逆转长期大剂量IFN-α诱导的与mPFC?vHi尤其是杏仁核局部明显神经炎症相关的抑郁样行为。芍药苷可能对IFN-α诱导的抑郁具有预防性治疗潜力。 (注:原文中“IL-6,IL-1β和TNF-α”以及“IL-9,IL-10,IL-12,和MCP-1”后的中文问号为原文未明确表述,保留疑问符号)